| pubmed-article:11133363 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11133363 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:11133363 | lifeskim:mentions | umls-concept:C0006104 | lld:lifeskim |
| pubmed-article:11133363 | lifeskim:mentions | umls-concept:C0205147 | lld:lifeskim |
| pubmed-article:11133363 | lifeskim:mentions | umls-concept:C0012929 | lld:lifeskim |
| pubmed-article:11133363 | lifeskim:mentions | umls-concept:C0205307 | lld:lifeskim |
| pubmed-article:11133363 | lifeskim:mentions | umls-concept:C0162735 | lld:lifeskim |
| pubmed-article:11133363 | lifeskim:mentions | umls-concept:C2587213 | lld:lifeskim |
| pubmed-article:11133363 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:11133363 | pubmed:dateCreated | 2001-2-22 | lld:pubmed |
| pubmed-article:11133363 | pubmed:abstractText | Recent observations in cultured human fibroblasts suggest that the accumulation of point mutations in the noncoding control region of mtDNA may be important in human aging. We studied the mtDNA control region in brain tissue from 31 normal elderly individuals, from 35 individuals who had Alzheimer disease, and from 47 individuals who had dementia with Lewy bodies. We found no evidence that these somatic mtDNA point mutations accumulate either in the brains of normal elderly individuals or in the brains of individuals with neurodegenerative disease. | lld:pubmed |
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| pubmed-article:11133363 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11133363 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11133363 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:11133363 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11133363 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:11133363 | pubmed:issn | 0002-9297 | lld:pubmed |
| pubmed-article:11133363 | pubmed:author | pubmed-author:BrownD TDT | lld:pubmed |
| pubmed-article:11133363 | pubmed:author | pubmed-author:HowellNN | lld:pubmed |
| pubmed-article:11133363 | pubmed:author | pubmed-author:TaylorG AGA | lld:pubmed |
| pubmed-article:11133363 | pubmed:author | pubmed-author:ParsonsT JTJ | lld:pubmed |
| pubmed-article:11133363 | pubmed:author | pubmed-author:TurnbullD MDM | lld:pubmed |
| pubmed-article:11133363 | pubmed:author | pubmed-author:ChinneryP FPF | lld:pubmed |
| pubmed-article:11133363 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11133363 | pubmed:volume | 68 | lld:pubmed |
| pubmed-article:11133363 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11133363 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11133363 | pubmed:pagination | 529-32 | lld:pubmed |
| pubmed-article:11133363 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:11133363 | pubmed:meshHeading | pubmed-meshheading:11133363... | lld:pubmed |
| pubmed-article:11133363 | pubmed:year | 2001 | lld:pubmed |
| pubmed-article:11133363 | pubmed:articleTitle | Point mutations of the mtDNA control region in normal and neurodegenerative human brains. | lld:pubmed |
| pubmed-article:11133363 | pubmed:affiliation | Department of Neurology, The Medical School, University of Newcastle upon Tyne, NE2 4HH, United Kingdom. P.F.Chinnery@newcastle.ac.uk | lld:pubmed |
| pubmed-article:11133363 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11133363 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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